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All procedures have been reviewed and approved by the Institutional Review Board of the Balearic Islands Health Service Research Ethics Committee (CEI-IB; Ref No: IB 5701\/25). Written informed consent will be obtained from all participants at the time of enrolment. All collected data will be anonymized and treated with strict confidentiality. Participants may voluntarily withdraw their informed consent at any time. Data collected prior to participant withdrawal will be retained and used for the conduct of the study as indicated in the informed consent. Data obtained through interviews and focus groups will be pseudonymised during the transcription process, and identifiable data will be removed to ensure participant confidentiality. The data obtained will be entered into a database, where the information concerning each participant will be directly anonymised after extraction from the clinical history. This information will remain under the custody of the principal investigators, and its access will be restricted to them, as well as to the collaborating investigators, who will sign a confidentiality document.Regarding the collection of data through qualitative methodology, candidates will be asked to participate, will be provided with a data collection sheet, and will be asked to complete a questionnaire. These procedures are subject to the provisions of Organic Law 3\/2018, of 5 December, on the protection of personal data and guarantee of digital rights.This is a non\u2011clinical implementation study in which no experimental clinical interventions are delivered to participants. No harms related to participation are expected, given the non\u2011interventional nature of the study. Therefore, no ancillary or post\u2011trial clinical care is planned beyond usual care routinely provided within the health system. No financial or other compensation for participation is offered. In the unlikely event that any harm attributable to study procedures were to occur, it would be managed in accordance with applicable institutional policies and standard healthcare procedures.The results of this study will be disseminated through multiple channels. Study findings will be reported in the trial registry (ClinicalTrials.gov) and submitted for publication in peer\u2011reviewed scientific journals, as well as presented at national and international conferences. A summary of the main results will be shared with participating PCCs and healthcare professionals through feedback sessions and institutional reports. In addition, a plain\u2011language summary of the findings will be made available to participating centres and relevant stakeholders to facilitate knowledge transfer and support future implementation.","order":1,"name":"Ethics","label":"Ethics approval and consent to participate","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"Not applicable.","order":2,"name":"Ethics","label":"Consent for publication","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The authors declare no competing interests.","order":3,"name":"Ethics","label":"Competing interests","group":{"name":"EthicsHeading","label":"Declarations"}}],"article-number":"318"}}